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Work in inVentiv Health for Sr. Clinical Data Manager

 

Clinical courses

 

Clinical courses

inVentiv Health Clinical, a leader in drug development services, has a global infrastructure, therapeutic expertise, and commitment to quality that is unmatched in the industry. For pharmaceutical, biotechnology, generic drug, and medical device companies of all sizes around the world, inVentiv Health Clinical can help you transform promising ideas into commercial reality.

Post: Sr. Clinical Data Manager

Job Description

  • Reports to InVentiv Health Clinical Senior Technical Global Team Leader of data management
  • May work as back up to Sr. Technical Global Team Leader of data management with InVentiv Health Clinical -India studies as needed. Manages the Data Managers and eCRF Developers/Database Designers on study related tasks with InVentiv Health Clinical -India site. Provides additional training and mentors InVentiv Health Clinical Data Managers.
  • Leads DM activities on assigned studies including performing activities from set-up for EDC studies to database freeze.
  • Monitors and adheres to study timeline as it relates to assigned activities.
  • Creates, reviews, and finalizes SVWT document.
  • Schedules SVWT meeting and drafts study setup timings as agreed upon by the clinical study sub-team (CSST).
  • Schedules screen reviewing meetings with CSST and eCRF developer.
  • Reviews and approves screens with input from CSST.
  • Reviews and approves Annotated eCRF.
  • Creates, sends for review, and approves eCRF completion guidelines.
  • Creates DVS and UAT test scripts in conjunction with eCRF developer; sends for review, and final approval.
  • Maintains eCRF Development Issue Log.
  • Performs DVS UAT documenting findings on the eCRF Development Issue Log.
  • Creates and sends Deployment UAT document for review and approval Runs and reviews data listings and reports.
  • Performs in-steam data cleaning activities: reviews subject data, reviews auto query responses and closes auto-queries, reviews and processes candidate queries, generates manual queries, and freezes subject casebooks.
  • Coordinates all coding activities from set up for final approval at study completion.
  • Performs database closeout activities: reconciles SAE, obtains medical term coding approval, reconciles external data, freezes casebooks, and declares database complete and frozen.
  • Designs, reviews and approves paper study documents.
  • Attends Data and Programming Operations, CSST, and other meetings as needed.
  • Works with and communicates with InVentiv Health Clinical as needed for assignments.

Candidate Profile

  • Bachelors degree in Life Sciences, Mathematics, Statistics, Computer Science or a Medical/Nursing qualification.
  • 5-7 years of experience into Data Management activities (DE Screen Testing, Edit Check Creation and Testing, Query Management, Data Entry guidelines creation, DB Lock/Unlock) in the pharmaceutical industry or a clinical/health-related research organization
  • Understanding of clinical trial methodology and GCP. 
  • Experience and understanding of at least one clinical data management system (e.g. Clintrial, Oracle Clinical).
  • Good verbal and written communication skills.
  • Ability to work on multiple projects, plan, organize and prioritize activities.
  • Knowledge of Framemaker, PL/SQL, Inform and/or EDC systems an additional plus.

Additional Information:
Qualification: Bachelor’s Degree in a life science or nursing
Job ID: 14294
Location: Pune

Industry Type: Clinical Research
Last Date: 21st December, 2016

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